75150-001 NDC - PRIMEAUTY ()

Drug Information

Product NDC: 75150-001

Proprietary Name: Primeauty

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Huizhou New Road Cosmetics Company Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	4/22/2020

No.	Package Code	Package Description
1	75150-001-01	240 mL in 1 BOTTLE, PUMP (75150-001-01)
2	75150-001-02	250 mL in 1 BOTTLE, PUMP (75150-001-02)
3	75150-001-03	300 mL in 1 BOTTLE, PUMP (75150-001-03)
4	75150-001-04	350 mL in 1 BOTTLE, PUMP (75150-001-04)
5	75150-001-05	400 mL in 1 BOTTLE, PUMP (75150-001-05)
6	75150-001-06	500 mL in 1 BOTTLE, PUMP (75150-001-06)
7	75150-001-07	1000 mL in 1 BOTTLE, PUMP (75150-001-07)

Field Name	Field Value	Definition
PRODUCT NDC	75150-001	The translation of the dosage form Code submitted by the firm.
PROPRIETARY NAME	Primeauty	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	Bottle (Pump)	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE	4/22/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Huizhou New Road Cosmetics Company Limited	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023